MedPath

Impact of Video Discharge Instructions on Heart Failure Patient's Knowledge

Not Applicable
Withdrawn
Conditions
Heart Failure
Interventions
Other: Video Discharge
Registration Number
NCT05908617
Lead Sponsor
Yasmeen Golzar
Brief Summary

With improve care of patients with heart failure, many patients are living longer. Care for these patients is now not only focused on mortality but also on the quality of life. Patient knowledge about heart failure and their overall compliance with the necessary lifestyle changes will lead to an improved quality of life. Discovering alternative ways to improve patient knowledge is key to long term survival. This studies objective is to assess the overall impact of video discharge instructions as compared to paper discharge instructions on Heart Failure Knowledge among an under-served patient population.

Detailed Description

In this study, we will randomized patients admitted to the hospital with heart failure exacerbation to receive either paper or video discharge instructions within a day prior to discharge. The video and paper instructions will have the same content. The patients will take a pre-test and post-test and the change in scores among the patients who received the video and paper discharge instructions will be compared. Other points of interest include participant satisfactions with discharge instruction, followup at post hospital appointment and 30-day readmission.

Data to be collected includes:

1. Medial history of the patient

2. Educational background

3. Social Status

4. Patients Health Measurement: Self Efficacy for managing medications and Treatment Management, Informational Support

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • hospital admission with a diagnosis of Heart Failure (HF)- Heart failure with reduced ejection fraction or heart failure with preserved Ejection fraction
  • planned discharge from hospital to home setting
  • able to read and write English
  • Acceptable to answer Questionnaire and to receive a call at the end of the study
Exclusion Criteria
  • Planned discharge to long term acute care
  • Patients with unstable housing
  • imprisoned patients
  • patients who are pregnant
  • illiteracy (defined as inability to write or read) and non-native speakers of English
  • impaired cognition
  • impaired vision
  • Patients with End Stage Renal Disease(ESRD)
  • Cancer patients

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Video Discharge InstructionsVideo DischargePatient will be given Video discharge instructions
Primary Outcome Measures
NameTimeMethod
Change in Heart Failure Knowledge Score1hr

Participants knowledge about heart failure will be assessed using the validated Atlanta Heart Failure Knowledge Test(AHFKT- V3). This is a test which includes 30 questions with a minimum score of 0 and a maximum score of 30. Each Participant will take the test and will subsequently be given either paper discharge instructions or both video and paper discharge instructions. After reading and/or watching the discharge instructions, each participant will take the same test once again. The difference in the pre and post intervention scores will be calculated and the investigators will assess if there is a significant difference in the mean change in score the control(Paper) vs. Intervention groups(Video).

Secondary Outcome Measures
NameTimeMethod
Post hospital followup rates30 days

Upon discharge from the hospital, Each participant is given a post hospital appointment within 14 days of the discharge date. We will assess the percentage of participates in both groups who come to post hospital appointments.

Participant Satisfaction with discharge Instructions1 day

Participant overall satisfaction with their discharge instructions will be assess using a 5 point likert scale which ranges from not at all helpful to extremely helpful

Heart Failure Readmission rates30days

Investigators will assess the percentage of participants in both groups who will be readmitted to the hospital within 30days after being discharged from the index visit.

Trial Locations

Locations (1)

John H Stroger Hospital

🇺🇸

Chicago, Illinois, United States

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